机译:通过PIFA介导的2-芳基烯胺酮的环氧化作用,通过氧化C-N键的形成合成咔唑酮和3-乙酰吲哚
Tianjin Key Laboratory for Modern Drug Deliver & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, P. R. China;
Tianjin Key Laboratory for Modern Drug Deliver & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, P. R. China;
Tianjin Key Laboratory for Modern Drug Deliver & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, P. R. China;
Tianjin Key Laboratory for Modern Drug Deliver & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, P. R. China;
Tianjin Key Laboratory for Modern Drug Deliver & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, P. R. China;
Tianjin Key Laboratory for Modern Drug Deliver & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, P. R. China;
机译:PIDA介导的分子内氧化C-N键形成,用于直接合成氨基尼喹啉
机译:通过C-N / N-S键形成合成5-氨基/氨基取代的1,2,4-噻唑的铜催化的有氧氧化[3 + 2]附片
机译:一锅合成的取代异噻唑-3(2H)-一:通过PIFA介导的N-S键形成的α-氨基甲酰基酮-S,S-缩醛的分子内环化。
机译:利用钯催化的C-C和C-N键形成反应在六元氧杂环的合成中
机译:掺杂剂铱络合物催化C-C(C-N)键合形成和C-O键切割
机译:通过串联C-H和N-H键官能无金属分子间氧化C-N键的形成
机译:纳米氧化亚铜催化一锅合成咔唑基STAT3抑制剂:通过分子内C-N键形成反应的简便方法